510(k) K021373 ยท MWJ Electrocardiograph, Ambulatory (Without Analysis)
H12+HOLTER RECORDER
| Applicant | Mortara Instrument, Inc., Milwaukee WI, US |
| Decision | Substantially Equivalent, Jun 27, 2002 |
| Received | May 1, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K021373
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.